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Megestrol Acetate - 17856-0907-2 - (Megestrol Acetate)

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Drug Information of Megestrol Acetate

Product NDC: 17856-0907
Proprietary Name: Megestrol Acetate
Non Proprietary Name: Megestrol Acetate
Active Ingredient(s): 40    mg/mL & nbsp;   Megestrol Acetate
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Megestrol Acetate

Product NDC: 17856-0907
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075671
Marketing Category: ANDA
Start Marketing Date: 20010725

Package Information of Megestrol Acetate

Package NDC: 17856-0907-2
Package Description: 20 mL in 1 CUP (17856-0907-2)

NDC Information of Megestrol Acetate

NDC Code 17856-0907-2
Proprietary Name Megestrol Acetate
Package Description 20 mL in 1 CUP (17856-0907-2)
Product NDC 17856-0907
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Megestrol Acetate
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20010725
Marketing Category Name ANDA
Labeler Name Atlantic Biologicals Corps
Substance Name MEGESTROL ACETATE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Megestrol Acetate


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